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m-Chloroperbenzoic acid → 6-Methanesulphonamido-2-methylquinoline-1-oxide

HRID 467104
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HRID 467104 반응식
ClC1C=CC=C(C(OO)=[O:9])C=1.[CH3:12][S:13]([NH:16][C:17]1[CH:18]=[C:19]2[C:24](=[CH:25][CH:26]=1)[N:23]=[C:22]([CH3:27])[CH:21]=[CH:20]2)(=[O:15])=[O:14]>C(Cl)Cl.C(=O)(O)[O-].[Na+]>[CH3:12][S:13]([NH:16][C:17]1[CH:18]=[C:19]2[C:24](=[CH:25][CH:26]=1)[N+:23]([O-:9])=[C:22]([CH3:27])[CH:21]=[CH:20]2)(=[O:14])=[O:15]
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참가 물질

5

반응물 2

HCID 70297m-Chloroperbenzoic acidHCID 19813426N-(2-Methylquinolin-6-yl)methanesulfonamide

생성물 1

HCID 198134366-Methanesulphonamido-2-methylquinoline-1-oxide

시약·촉매·용매 2

HCID 6344Dichloromethane용매HCID 516892Sodium Bicarbonate용매

실험 절차

m-Chloroperbenzoic acid ("MCPBA") (5.2 g) was added portionwise to a solution of 6-methanesulphonamido-2-methylquinoline (6 g) in methylene chloride and stirring was continued for 17 hours. The reaction mixture was then diluted with aqueous sodium bicarbonate and the organic layer was separated. The aqueous layer was extracted with methylene chloride. The combined organic layers were washed with aqueous sodium bicarbonate, dried (MgSO4) and evaporated in vacuo to give a solid which was recrystallised from ethanol to give the title compound, yield 1.6 g, m.p. 241°-243°.

후처리

  1. customthe organic layer was separated
  2. extractionThe aqueous layer was extracted with methylene chloride
  3. washThe combined organic layers were washed with aqueous sodium bicarbonate
  4. dry with materialdried (MgSO4)
  5. customevaporated in vacuo
  6. customto give a solid which
  7. customwas recrystallised from ethanol

출처 및 근거

ORD 기록
ord-d93894f0ebc546c89f1b63da77f6b7af
출처 데이터셋
uspto-grants-1992_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05158964

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